Dexlido Kit
Product Images NDC 76420-767

4 FDA label images from Asclemed Usa, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dexlido Kit (NDC 76420-767). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Dexamethasonestructure (Dex0a 0004 01)

Dexamethasonestructure (Dex0a 0004 01)
Chemical structure diagram of the active ingredient dexamethasone sodium phosphate, showing molecular formula C22H28FNa2O8P and molecular weight 516.41.*
FDA Label Image

Logo (Dex0a 0004 02)

FDA Label Image

Structural Formula Lidocaine Hydrochloride (Dex0a 0004 03)

Structural Formula Lidocaine Hydrochloride (Dex0a 0004 03)
Chemical structure diagram depicting a molecule likely related to one of the active ingredients in Dexlido Kit, which contains Dexamethasone Sodium Phosphate, Lidocaine Hydrochloride, and Povidine Iodine. The structure shows a benzene ring with two methyl groups and an amide side chain with hydrochloride and hydrate components.*
FDA Label Image

Principal Display Panel – Kit Label (Dex0a 0004 04)

Principal Display Panel – Kit Label (Dex0a 0004 04)
Dexlido Kit packaging label showing the product name prominently. The label lists kit contents including Dexamethasone Sodium Phosphate Injection 10mg/mL (1mL), Lidocaine HCl Injection 1% Ampule (2mL), Povidone-Iodine swabsticks, isopropyl alcohol prep pads, sterile gloves, drape, adhesive bandage, and non-sterile gauze. It indicates needles and syringes are not included. Distributed by Enovacchem Pharmaceuticals, Torrance, CA. Rx Only.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.